SI
SI
discoversearch

We've detected that you're using an ad content blocking browser plug-in or feature. Ads provide a critical source of revenue to the continued operation of Silicon Investor.  We ask that you disable ad blocking while on Silicon Investor in the best interests of our community.  If you are not using an ad blocker but are still receiving this message, make sure your browser's tracking protection is set to the 'standard' level.
Strategies & Market Trends : Stock Watcher's Thread / Pix of the Week (POW) -- Ignore unavailable to you. Want to Upgrade?


To: John M. who wrote (10320)6/10/1999 10:16:00 AM
From: RCJIII  Read Replies (1) | Respond to of 52051
 
This is big, everyone check out this news-

NERX-

(BSNS WIRE) NeoRx's Pretarget-Lymphoma Produces Tumor Regressions, Inclu
NeoRx's Pretarget-Lymphoma Produces Tumor Regressions, Including Complete
Responses; Data Selected for 'Highest Grade' in Therapeutic Oncology at Society
of Nuclear Medicine


Business Editors

LOS ANGELES--(BUSINESS WIRE)--June 10, 1999--Dr. Hazel Breitz,
Virginia Mason Medical Center (Seattle, WA), reported at the Society
of Nuclear Medicine meeting that NeoRx Corporation's (Nasdaq:NERX)
Pretarget(R) technology permitted the safe administration of higher
radiation doses to lymphoma patients than conventional
radioimmunotherapy, and that patients receiving these doses
experienced substantial tumor regressions including complete responses
in some cases. The maximum tolerated dose has not yet been reached.
The abstract describing this work received the highest grade in the
category of Therapeutic Oncology at the meeting.
"Both dosimetry calculations and the patients' tolerance and
responses provide proof-of-concept that Pretarget technology may
provide substantial benefits to lymphoma patients, even some who have
had extensive prior therapies such as bone marrow transplantation,"
said Dr. Breitz.
The Pretarget technology employed involves first injecting a
tumor-directed antibody carrying a receptor to the tumor, followed by
a clearing step to remove the receptor from circulation. The radiation
is then injected on a small molecule carrier that rapidly targets the
receptor on the tumor, with most of the remaining radiation being
quickly excreted from the body. By contrast, conventional approaches
attach the radiation to the antibody that circulates throughout the
body for a sustained period, increasing the radiation exposure to
normal organs such as bone marrow.
Patients involved in this proof-of-concept study included both
intermediate and low-grade lymphoma patients, most of whose tumors had
grown again after extensive prior therapies. Three patients had
received high dose therapy requiring bone marrow transplantation;
other patients had bone marrow that was extensively involved with
tumor. "It is remarkable, but not surprising, that even these patients
tolerated these high doses well, and it is particularly gratifying
that one of the complete responses was achieved in a patient who had
received a prior stem cell transplant," said Paul Abrams, M.D., J.D,
NeoRx's Chief Executive Officer. "That is what this work is all about.
Although this study was conducted with a commercially-available
lymphoma antibody, NeoRx has now constructed its own proprietary
molecule designed to improve binding to lymphoma cells and that may
result in reduced manufacturing lead times and costs."
NeoRx Corporation is developing innovative products designed to
provide improved, cost-effective treatments for patients with cancer
and inflammatory diseases.
This release contains forward-looking statements relating to the
development of the Company's products and future operating results
that are subject to certain risks and uncertainties that could cause
actual results to differ materially from those projected. The words
"may," "believe," "expect," "intend," "anticipate," variations of such
words, and similar expressions identify forward-looking statements,
but their absence does not mean that the statement is not
forward-looking. These statements are not guarantees of future
performance and are subject to certain risks, uncertainties and
assumptions that are difficult to predict. Factors that could affect
the Company's actual results include the progress and costs of
clinical trials and the timing of regulatory approvals. Reference is
made to the Company's latest Annual Report on Form 10 - K filed with
the Securities and Exchange Commission for a more detailed description
of such factors. Readers are cautioned not to place undue reliance on
these forward-looking statements that speak only as of the date of
this release. The Company undertakes no obligation to publicly update
any forward-looking statement to reflect new information, events or
circumstances after the date of this release or to reflect the
occurrence of unanticipated events.
Visit NeoRx at www.neorx.com.
To receive NeoRx news releases via email, register at
www.neorx.com/news/pr.html.

NeoRx and Pretarget are trademarks or registered trademarks of
NeoRx Corporation in the United States and/or foreign countries.
(c) 1999 NeoRx Corporation. All Rights Reserved.

--30--APS/se*

CONTACT: NeoRx
Melinda Kile, 206/286-2508
Controller

KEYWORD: WASHINGTON CALIFORNIA
INDUSTRY KEYWORD: PHARMACEUTICALS MEDICINE BIOTECHNOLOGY
Today's News On The Net - Business Wire's full file on the Internet
with Hyperlinks to your home page.
URL: businesswire.com




*** end of story ***